National Drug Code (NDC) Database
ANIMEX FOODS SP Z O O ODDZIAL W STARACHOWICACH
-
NDC:
72666-2022
-
Nonproprietary Name:
Crude Heparin
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
HEPARIN SODIUM
-
Start Marketing Date:
2022-04-01
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
Anna Lotan Ltd
-
NDC:
76446-047
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
LOTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
210 mg/g
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2024-11-19
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Anonima Materie Sintetiche and Affini (AMSA) Spa
-
NDC:
17373-1446
-
Nonproprietary Name:
Amantadine Hydrochloride
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
AMANTADINE HYDROCHLORIDE
-
Start Marketing Date:
2014-10-27
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Anqiu Lu'an Pharmaceutical Co. Ltd
-
NDC:
59644-9915
-
Nonproprietary Name:
Acetaminophen/Diphenhydramine
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2010-11-17
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Anqiu Lu'an Pharmaceutical Co., Ltd.
-
NDC:
59644-9933
-
Nonproprietary Name:
Acetaminophen DC90-22
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2022-07-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Anqui Lu'an Pharmaceutical Co.,Ltd.
-
NDC:
59644-9004
-
Nonproprietary Name:
Acetaminophen DC90-3
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2017-09-13
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Antaria Pty Ltd
-
NDC:
83679-1016
-
Nonproprietary Name:
Zinc Oxide
-
Dosage Form:
SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
85 kg/100kg
-
Substance:
ZINC OXIDE
-
Start Marketing Date:
2021-09-07
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2027-12-31
-
NDC:
23639-0003
-
Nonproprietary Name:
Valproic Acid
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
VALPROIC ACID
-
Start Marketing Date:
2006-01-10
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
59644-9922
-
Nonproprietary Name:
Acetaminophen
-
Dosage Form:
POWDER
-
Product Type:
BULK INGREDIENT
-
Strength:
1 kg/kg
-
Substance:
ACETAMINOPHEN
-
Start Marketing Date:
2016-04-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
-
NDC:
51858-001
-
Nonproprietary Name:
SODIUM MOLYBDATE
-
Dosage Form:
SOLUTION
-
Product Type:
DRUG FOR FURTHER PROCESSING
-
Strength:
156 mg/mL
-
Substance:
SODIUM MOLYBDATE MO-99
-
Start Marketing Date:
2013-08-14
-
End Marketing Date:
0000-00-00
-
DEA Schedule:
-
Certified Through:
2026-12-31
Create a New Buying Request
Fields marked with * are mandatory.